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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Soumeya Bekri

Department of Biochemistry

Centre Hospitalier Universitaire de Nice

France

[email]@chu-nice.fr

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Biochemistry, Centre Hospitalier Universitaire de Nice, France. 2004 - 2005

References

  1. Fabry disease in patients with end-stage renal failure: the potential benefits of screening. Bekri, S., Enica, A., Ghafari, T., Plaza, G., Champenois, I., Choukroun, G., Unwin, R., Jaeger, P. Nephron. Clin. Pract (2005) [Pubmed]
  2. Early diagnosis of mucopolysaccharidosis III A with a nonsense mutation and two de novo missense mutations in SGSH gene. Bekri, S., Armana, G., De Ricaud, D., Osenda, M., Maire, I., Van Obberghen, E., Froissart, R. J. Inherit. Metab. Dis. (2005) [Pubmed]
  3. The molecular basis of succinic semialdehyde dehydrogenase deficiency in one family. Bekri, S., Fossoud, C., Plaza, G., Guenne, A., Salomons, G.S., Jakobs, C., Van Obberghen, E. Mol. Genet. Metab. (2004) [Pubmed]
 
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